Abstract
Aquatic invertebrates of groundwater-dependent wetlands can be sensitive to a drop in the groundwater table, which is considered one of the possible impacts of climate change. We investigated whether aquatic clitellate species are able to dwell in waterlogged substrates without surface water, in 27 spring fens studied across the Western Carpathians. A total of 78 clitellate species were recorded in pairs of samples from aquatic and semi-aquatic habitats. Semi-aquatic habitats had 27 species in common with aquatic habitats, but algal and fungal feeders were less frequent and abundant, and predatory leeches and Haplotaxis gordioides completely lacking. Terrestrial enchytraeid species enriched the semi-aquatic assemblages. The main change in clitellate composition was controlled by total organic carbon. The importance of further variables, however, differed between aquatic and semi-aquatic sites. Further analyses of semi-aquatic sites showed that the distribution of primarily aquatic species was mainly driven by physical and chemical variables, while that of soil dwellers was driven by depth. Except Tubifex tubifex and Nais communis, all aquatic species preferred the uppermost layer. Results indicate that, during extreme droughts, when aquatic habitats cease to exist, some aquatic clitellates can persist in the waterlogged substrate, while some aquatic specialists may face the risk of local extinction.
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References
Barquín, J. & M. Scarsbrook, 2008. Management and conservation strategies for coldwater springs. Aquatic Conservation Marine and Freshwater Ecosystems 18: 580–591.
Bertrand, G., N. Goldscheider, J.-M. Gobat & D. Hunkeler, 2012. Review: from multi-scale conceptualization to a classification system for inland groundwater-dependent ecosystems. Hydrogeology Journal 20: 5–25.
Bojková, J., J. Schenková, M. Horsák & M. Hájek, 2011. Species richness and composition patterns of clitellate (Annelida) assemblages in the treeless spring fens: the effect of water chemistry and substrate. Hydrobiologia 677: 159–171.
Briones, M. J. I., P. Ineson & T. G. Piearce, 1997. Effects of climate change on soil fauna; responses of enchytraeids, Diptera larvae and tardigrades in a transplant experiment. Applied Soil Ecology 6: 117–134.
Cantonati, M., L. Füreder, R. Gerecke, I. Jüttner & E. J. Cox, 2012. Crenic habitats, hotspots for freshwater biodiversity conservation: toward an understanding of their ecology. Freshwater Science 31: 463–480.
Cragg, J. B., 1961. Some aspects of the ecology of moorland animals. Journal of Ecology 49: 477–506.
Dawson, T. P., P. M. Berry & E. Kampa, 2003. Climate change impacts on freshwater wetland habitats. Journal for Nature Conservation 11: 25–30.
Dumnicka, E., 2000. Studies on Oligochaeta taxocens in streams, interstitial and cave waters of southern Poland with remarks on Aphanoneura and Polychaeta distribution. Acta Zoologica Cracoviensia 43: 339–392.
Dumnicka, E., 2001. Some remarks on the origin of stygobiontic oligochaetes. Mémoires de Biospéleologie 28: 39–45.
Erman, D. C. & N. A. Erman, 1975. Macroinvertebrate composition and production in some Sierra Nevada minerotrophic peatlands. Ecology 56: 591–603.
Erséus, C., M. J. Wetzel & L. Gustavsson, 2008. ICZN rules—a farewell to Tubificidae (Annelida, Clitellata). Zootaxa 1744: 66–68.
ESRI, 2003. ArcGIS 8.3. Environmental Systems Research Institute, Redlands, CA, USA, http://www.esri.com.
Giere, O., 1993. Meiobenthology, the Microscopic Fauna in Aquatic Sediments. Springer, Berlin Heidelberg.
Glazier, D. S., 1991. The fauna of North American temperate cold springs: patterns and hypotheses. Freshwater Biology 26: 527–542.
Gower, J. C., 1975. Generalized procrustes analysis. Psychometrika 40: 33–51.
Graefe, U. & R. M. Schmelz, 1999. Indicator values, strategy types and life forms of terrestrial Enchytraeidae and other microannelids. In Schmelz R. M. & Sühlo K. (eds), Proceedings of the 3rd International Symposium on Enchytraeidae, Osnabrück, Germany: 3–4 July 1998, Universitätsverlag Rasch, Osnabrück (Newsletter on Enchytraeidae 6): 59–67.
Green, T. R., M. Taniguchi, H. Kooi, J. J. Gurdak, D. M. Allen, K. M. Hiscock, H. Treidel & A. Aureli, 2011. Beneath the surface of global change: impacts of climate change on groundwater. Journal of Hydrology 405: 532–560.
Hájek, M. & P. Hekera, 2004. Can seasonal variation in fen water chemistry influence the reliability of vegetation-environment analyses? Preslia 76: 1–14.
Hájek, M., P. Hekera & P. Hájková, 2002. Spring fen vegetation and water chemistry in the Western Carpathian flysch zone. Folia Geobotanica 37: 205–224.
Hájek, M., P. Hájková, K. Rybníček & P. Hekera, 2005. Present vegetation of spring fens and its relation to water chemistry. In Poulíčková, A., M. Hájek & K. Rybníček (eds), Ecology and Palaeoecology of Spring Fens of the West Carpathians. Palacký University, Olomouc: 69–96.
Hájek, M., M. Horsák, P. Hájková & D. Dítě, 2006. Habitat diversity of central European fens in relation to environmental gradients and an effort to standardise fen terminology in ecological studies. Perspectives in Plant Ecology, Evolution and Systematics 8: 97–114.
Hannigan, E. & M. Kelly-Quinn, 2012. Composition and structure of macroinvertebrate communities in contrasting open-water habitats in Irish peatlands: implications for biodiversity conservation. Hydrobiologia 692: 19–28.
Healy, B., 1987. The depth distribution of Oligochaeta in an Irish quaking marsh. Hydrobiologia 155: 235–247.
Healy, B. & T. Bolger, 1984. The occurrence of species of semi-aquatic Enchytraeidae (Oligochaeta) in Ireland. Hydrobiologia 115: 159–170.
Horsák, M., V. Rádková, J. Bojková, V. Křoupalová, J. Schenková, V. Syrovátka & J. Zajacová, 2015. Drivers of aquatic macroinvertebrate richness in spring fens in relation to habitat specialization and dispersal mode. Journal of Biogeography 42: 2112–2121.
Horsák, M., V. Polášková, M. Zhai, J. Bojková, V. Syrovátka, V. Šorfová, J. Schenková, M. Polášek, T. Peterka & M. Hájek, 2018. Spring-fen habitat islands in a warming climate: partitioning the effects of mesoclimate air and water temperature on aquatic and terrestrial biota. Science of the Total Environment 634: 355–365.
Hrabě, S., 1942. Poznámky o zvířeně ze studní a pramenů na Slovensku. Sborník Přírodovědeckého klubu v Brně 24: 23–30.
IPCC, 2014. Climate change 2014—impacts, adaptation and vulnerability: regional aspects. Cambridge University Press, New York.
Jackson, D. A., 1995. PROTEST: a PROcrustean randomization TEST of community environment concordance. Écoscience 2: 297–303.
Juget, J. & M. Lafont, 1994. Theoretical habitat templets, species traits, and species richness: aquatic oligochaetes in the Upper Rhône River and its floodplain. Freshwater Biology 31: 327–340.
Kløve, B., P. Ala-Aho, G. Bertrand, J. J. Gurdak, H. Kupfersberger, J. Kværner, T. Muotka, H. Mykrä, E. Preda, P. Rossi, C. B. Uvo, E. Velasco & M. Pulido-Velazquez, 2014. Climate change impacts on groundwater and dependent ecosystems. Journal of Hydrology 518: 250–266.
Košel, V., 2001. Hirudinológia pre hydrobiológov v praxi. In Makovinská, J. & L. Tóthová (eds), Zborník z hydrobiologického kurzu 2001. Rajecké Teplice: 37–54.
Křoupalová, V., J. Bojková, J. Schenková, P. Pařil & M. Horsák, 2011. Small-scale distribution of aquatic macroinvertebrates in two spring fens with different groundwater chemistry. International Review of Hydrobiology 96: 235–256.
Laiho, R., N. Silvan, H. Cárcamo & H. Vasander, 2001. Effects of water level and nutrients on spatial distribution of soil mesofauna in peatlands drained for forestry in Finland. Applied Soil Ecology 16: 1–9.
Learner, M. A., G. Lochhead & B. D. Hughes, 1978. A review of the biology of British Naididae (Oligochaeta) with emphasis on the lotic environment. Freshwater Biology 8: 357–375.
Martínez-Ansemil, E. & R. Collado, 1996. Distribution patterns of aquatic oligochaetes inhabiting watercourses in the Northwestern Iberian Peninsula. Hydrobiologia 334: 73–83.
Martinsson, S., E. Rota & C. Erséus, 2015a. Revision of Cognettia (Clitellata, Enchytraeidae): re-estabilishment of Chamaedrilus and description of cryptic species in the sphagnetorum complex. Systematics and Biodiversity 13: 257–277.
Martinsson, S., E. Rota & C. Erséus, 2015b. On the identity of Chamaedrilus glandulosus (Michaelsen, 1881) (Clitellata, Enchytraeidae), with the description of a new species. Zookeys 501: 1–14.
Neubert, E. & H. Nesemann, 1999. Annelida, Clitellata; Branchiobdellida, Acanthobdellea, Hirudinea. Spektrum Akademischer Verlag, Berlin.
Nijboer, R. C., M. J. Wetzel & P. F. M. Verdonschot, 2004. Diversity and distribution of Tubificidae, Naididae, and Lumbriculidae (Annelida: Oligochaeta) in the Netherlands: an evaluation of 20 years of monitoring data. Hydrobiologia 520: 127–141.
Oksanen, J., F. G. Blanchet, M. Friendly, R. Kindt, P. Legendre, D. McGlinn, P. R. Minchin, R. B. O’Hara, G. L. Simpson, P. Solymos, M. Henry, H. Stevens, E. Szoecs & H. Wagner, 2017. vegan: Community ecology package. 2013. R-package version 2.4–3. Available at: http://CRAN.R-project.org/package=vegan.
Omesová, M. & J. Helešic, 2004. On the processing of freeze-core samples with notes on the impact of sample size. Scripta Facultatis Scientiarum Naturalium Universitatis Masarykianae Brunensis. Biology. Studies in Hydrobiology 29: 59–66.
Pižl, V., 2002. Žížaly České republiky. Earthworms of the Czech Republic, Sborník přírodovědeckého klubu v Uherském Hradišti, Supp: 9.
Plum, N. M. & J. Filser, 2005. Floods and drought: Response of earthworms and potworms (Oligochaeta: Lumbricidae, Enchytraeidae) to hydrological extremes in wet grassland. Pedobiologia 49: 443–453.
Prendergast-Miller, M., V. Standen, I. D. Leith & L. J. Sheppard, 2009. Response of enchytraeid worm populations to different forms of nitrogen (ammonia, ammonium, and nitrate) deposition. Soil Organisms 81: 225–236.
R Development Core Team, 2015. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/.
Rádková, V., V. Syrovátka, J. Bojková, J. Schenková, V. Křoupalová & M. Horsák, 2014. The importance of species replacement and richness differences in small-scale diversity patterns of aquatic macroinvertebrates in spring fens. Limnologica 47: 52–61.
Richards, K. S., 1977. Structure and function in the oligochaete epidermis (Annelida). Symposia of the Zoological Society of London 39: 171–193.
Römbke, J., J.-P. Sousa, T. Schouten & F. Riepert, 2006. Monitoring of soil organisms: a set of standardized field methods proposed by ISO. European Journal of Soil Biology 42: 61–64.
Sawyer, R. T., 1986. Leech Biology and Behaviour, Vol. II. Clarendon Press, Oxford.
Schenková, J., M. Bílková & M. Horsák, 2016. The response of Clitellata (Annelida) to environmental gradients in spring fens. Limnologica 57: 73–82.
Schmelz, R. M. & R. Collado, 2010. A guide to European terrestrial and freshwater species of Enchytraeidae (Oligochaeta). Soil Organisms 82: 1–176.
Schmelz, R. M., R. Collado & J. Römbke, 2015. Cognettia Nielsen & Christensen, 1959 (Annelida, Oligochaeta, enchytraeidae): proposed precedence over Euenchytraeus Bretscher, 1906 and Chamaedrilus Friend, 1913. The Bulletin of Zoological Nomenclature 72: 186–192.
Schwank, P., 1981. Turbellarien, Oligochaeten und Archianneliden des Breitenbachs und anderer oberhessischer Mittelgebirgsbäche. II. Die Systematik und Autökologie der einzelnen Arten. Schlitzer Produktionsbiologische Studien (43-2). Archiv für Hydrobiologie, Supplement 62: 86–147.
Seys, J., M. Vincx & P. Meire, 1999. Spatial distribution of oligochaetes (Clitellata) in the tidal freshwater and brackish parts of the Schelde estuary (Belgium). Hydrobiologia 406: 119–132.
Silvan, N., R. Laiho & H. Vasander, 2000. Changes in mesofauna abundance in peat soils drained for forestry. Forest Ecology and Management 133: 127–133.
Smith, M. E. & J. R. Kaster, 1986. Feeding habits and dietary overlap of Naididae (Oligochaeta) from a bog stream. Hydrobiologia 137: 193–201.
Springett, J. A., J. E. Brittain & B. P. Springett, 1970. Vertical movement of Enchytraeidae (Oligochaeta) in moorland soils. Oikos 21: 16–21.
Standen, V., 1982. Associations of Enchytraeidae (Oligochaeta) in experimentally fertilized grasslands. Journal of Animal Ecology 51: 501–522.
Svendsen, J. A., 1957a. The distribution of Lumbricidae in an area of Pennine moorland. Journal of Animal Ecology 26: 411–421.
Svendsen, J. A., 1957b. The behaviour of lumbricids under moorland conditions. Journal of Animal Ecology 26: 423–439.
Terhivuo, J. & A. Saura, 2006. Dispersal and clonal diversity of North-European parthenogenetic earthworms. Biological Invasions 8: 1205–1218.
Timm, T., 2009. A guide to the freshwater Oligochaeta and Polychaeta of Northern and Central Europe. Lauterbornia 66: 1–235.
Tolasz, R., 2007. Climate Atlas of Czechia. Český hydrometeorologický ústav Olomouc. Univerzita Palackého v Olomouci, Olomouc.
van Asselen, S., P. H. Verburg, J. E. Vermaat & J. H. Janse, 2013. Drivers of wetland conversion: a global meta-analysis. PLoS ONE 8(11): e81292.
van Duinen, G. A., T. Timm, A. J. P. Smolders, A. M. T. Brock & W. C. E. P. Verberk, 2006. Differential response of aquatic oligochaete species to increased nutrient availability—a comparative study between Estonian and Dutch raised bogs. Hydrobiologia 564: 143–155.
von Fumetti, S., F. W. Wigger & P. Nagel, 2017. Temperature variability and its influence on macroinvertebrate assemblages of alpine springs. Ecohydrology 10: 1–9.
Verdonschot, P. F. M., 2007. Spatial and temporal re-distribution of Naididae (tubificoid naidids and naidids s.str., Annelida, Clitellata) in Europe due to climate change: a review based on observational data. Acta Hydrobiologica Sinica 31: 116–138.
Vu, V. Q., 2011. Ggbiplot: a ggplot2 based biplot. R Package. Version: 0.55. Available at: https://github.com/vqv/ggbiplot.
Acknowledgements
We would like to thank Vít Syrovátka and Marek Polášek for their help with the visualization of the results, and Ondřej Hájek for the preparation of the map. The study was supported by research grants of the Czech Science Foundation (GA15-15548S and GA16-03881S) and by the institutional support of the Masaryk University for PhD students.
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Schenková, J., Bílková, M., Polášková, V. et al. Variation of Clitellata (Annelida) assemblages related to water saturation in groundwater-dependent wetlands. Hydrobiologia 823, 49–65 (2018). https://doi.org/10.1007/s10750-018-3695-8
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DOI: https://doi.org/10.1007/s10750-018-3695-8